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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Trifluoroacetic acid methylene chloride → N-(4-fluoro-2-methylphenyl)azetidin-3-amine

HRID 72425
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반응식

HRID 72425 반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][CH:9]2[CH2:12][N:11](C(OC(C)(C)C)=O)[CH2:10]2)=[C:4]([CH3:20])[CH:3]=1.FC(F)(F)C(O)=O.ClCCl>ClCCl>[F:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][CH:9]2[CH2:12][NH:11][CH2:10]2)=[C:4]([CH3:20])[CH:3]=1
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참가 물질

4

반응물 2

HCID 21863450Trifluoroacetic acid methylene chlorideHCID 63303297Tert-butyl 3-((4-fluoro-2-methylphenyl)amino)azetidine-1-carboxylate

생성물 1

HCID 65958632N-(4-fluoro-2-methylphenyl)azetidin-3-amine수율 98.5%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To an ice cooled solution of tert-butyl 3-((4-fluoro-2-methylphenyl)amino)azetidine-1-carboxylate (D30) (300 mg, 1.07 mmol) in dichloromethane (2 ml), a mixture of trifluoroacetic acid/dichloromethane (4.5 ml/1.5 ml) was added and the mixture stirred at room temperature for 1 h. Solvents were evaporated in vacuo and the resulting residue was purified by SPE-SCX cartridge (10 g). Collected ammonia fractions, after solvent evaporation afforded the title compound (D55) (0022/107/1) (190 mg)

후처리

  1. additionwas added
  2. customSolvents were evaporated in vacuo
  3. customthe resulting residue was purified by SPE-SCX cartridge (10 g)
  4. customCollected ammonia fractions, after solvent evaporation

출처 및 근거

ORD 기록
ord-5184a9bd74214ac4abe69de265c0ac4e
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08828987B2

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